15+ Years Pharma Expertise

GMP & Regulatory Consulting Services for Pharmaceutical Industry

Design to Commissioning of Plants | QMS Establishment | Global Regulatory Approvals

Who We Are

QBridge is a GMP Consultancy services based in Vadodara, Gujarat, India. Our focus is on GMPs, but we cover so much more than that. We offer a broad range of services from Plant Design & Set up consultancy for Green Field Projects & Brown Field Enhancement, Qualification & Validation Services, GMP & Regulatory Consultancy with Audit and their Compliance Services, Contract Manufacturing, Loan Licence and P2P Product Manufacturing Services, Formulation, Analytical and Dossier Services, Training & Placement Services.

We are professionals having 15+ years of experience in pharmaceutical industry across domestic and international markets. Our experience spans from small, mid-sized to multi-national companies.

Our Core Services

QBridge Pharma offers comprehensive pharmaceutical consulting solutions to support compliance, quality systems, validation and regulatory approvals across domestic and international markets. Our services are designed to help pharmaceutical companies meet global regulatory expectations with confidence and efficiency.

Plant Design & Setup

GMP-compliant plant layout, facility design, greenfield and brownfield project support aligned with global regulatory standards.

Qualification & Validation

Complete equipment, system, process and facility qualification & validation services as per WHO, EU-GMP and ISO guidelines

GMP & Regulatory Consulting

Expert guidance for GMP compliance, regulatory approvals, gap analysis, inspections and authority interactions across global markets.

GMP Audits & Compliance

Third-party audits Mock regulatory audits Vendor & supplier audits

Contract & Loan Licence Manufacturing

Support for contract manufacturing, loan licence and P2P manufacturing with EU-GMP / WHO-GMP certified facilities.

Formulation & Dossier Services

Formulation development, analytical validation, CTD/eCTD dossier preparation, DMF filing and regulatory submissions.

Why Choose Us

15+ years of Regulatory & GMP experience. Experience across multiple dosage forms (Injectables, Solid Oral, Liquid Oral, Oncology, Cephalosporin etc.). End-to-end pharma consulting under one roof. Domestic & International Regulatory Expertise. Strong compliance & documentation support

Our Work Across GMP & Regulatory Projects

Explore a snapshot of our successfully executed pharmaceutical consulting projects. Our portfolio reflects hands-on experience in plant design, validation, GMP compliance, audits, and regulatory approvals across diverse dosage forms and global markets.

Each project demonstrates our commitment to quality, regulatory excellence, and client success.

"Reliable GMP & Regulatory Partner"

QBridge Pharma supported us in GMP gap analysis, validation, and inspection readiness. Their regulatory knowledge and practical approach helped us clear audits smoothly. A highly dependable consultancy for pharmaceutical compliance.

Head, Quality Assurance

Pharmaceutical Manufacturing Company

Ready to Start Your GMP & Regulatory Journey with Us?

Partner with QBridge Pharma for expert GMP consulting, regulatory compliance, validation, and approval support tailored to your business goals.

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